Page last updated: 2024-09-05

2',6'-dihydroxy-4'-methoxydihydrochalcone and 5,7-dimethoxyflavone

2',6'-dihydroxy-4'-methoxydihydrochalcone has been researched along with 5,7-dimethoxyflavone in 2 studies

Compound Research Comparison

Studies
(2',6'-dihydroxy-4'-methoxydihydrochalcone)
Trials
(2',6'-dihydroxy-4'-methoxydihydrochalcone)
Recent Studies (post-2010)
(2',6'-dihydroxy-4'-methoxydihydrochalcone)
Studies
(5,7-dimethoxyflavone)
Trials
(5,7-dimethoxyflavone)
Recent Studies (post-2010) (5,7-dimethoxyflavone)
110564038

Protein Interaction Comparison

ProteinTaxonomy2',6'-dihydroxy-4'-methoxydihydrochalcone (IC50)5,7-dimethoxyflavone (IC50)
Broad substrate specificity ATP-binding cassette transporter ABCG2Homo sapiens (human)9.2

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wanich, S; Yenjai, C1
Dong, JJ; Feng, YT; He, J; Lin, WQ; Lu, CL; Ouyang, H; Peng, ZY; Wang, JX; Xiang, YP; Xiao, ZP; Zhu, HL1

Other Studies

2 other study(ies) available for 2',6'-dihydroxy-4'-methoxydihydrochalcone and 5,7-dimethoxyflavone

ArticleYear
Cytotoxicity against KB and NCI-H187 cell lines of modified flavonoids from Kaempferia parviflora.
    Bioorganic & medicinal chemistry letters, 2010, May-01, Volume: 20, Issue:9

    Topics: Antineoplastic Agents; Benzopyrans; Cell Line, Tumor; Flavonoids; Humans; Oximes; Zingiberaceae

2010
Synthesis, structure-activity relationship analysis and kinetics study of reductive derivatives of flavonoids as Helicobacter pylori urease inhibitors.
    European journal of medicinal chemistry, 2013, Volume: 63

    Topics: Bacterial Proteins; Binding Sites; Binding, Competitive; Crystallography, X-Ray; Dose-Response Relationship, Drug; Enzyme Inhibitors; Flavonoids; Helicobacter pylori; Kinetics; Models, Chemical; Models, Molecular; Molecular Conformation; Molecular Structure; Oxidation-Reduction; Protein Binding; Protein Structure, Tertiary; Structure-Activity Relationship; Urease

2013